Demulsified extended life functional fluid

ABSTRACT

Functional fluid lubricating oil compositions are provided which comprise (A) a major amount of an oil of lubricating viscosity, and (B) an effective amount of each of the following: (1) an alkyl succinimide, (2) a Group II metal salt of a dihydrocarbyl dithiophosphoric acid, (3) a hydroxy fatty acid ester of a dihydric or polyhydric alcohol or oil-soluble alkoxylated derivatives thereof, and (4) a Group II metal salt of a hydrocarbyl sulfonic acid. Such lubricating compositions are useful as functional fluids in systems requiring fluid coupling, hydraulic fluid and/or lubrication of relatively moving parts. The lubricating compositions of the invention are particularly useful as the functional fluid in automatic transmissions, particularly in passenger automobiles. In addition, the fluids do not form stable emulsions with water.

United States Patent 1 [111 B 3,920,562

Foehr 14 Nov. 18, 1975 1 DEMULSIFIED EXTENDED LIFE 3,796,662 3/1974 Lyle et a1 252/51.5 A x FUNCTIONAL FLUID 3,850,455 9/1958 Kern et al. 252/33.4 X

[75] Inventor: Edward G. Foehr, San Rafael, Calif.

[73] Assignee: Chevron Research Company, San

Francisco, Calif.

[22] Filed: Feb. 5, 1973 [21] Appl. No.: 329,476

[44] Published under the Trial Voluntary Protest Program on January 28, 1975 as document no.

[52] US. Cl 252/32.7 E; 252/33.4; 252/75 [51] Int. Cl. C10M l/48 [58] Field of Search 252/37.7 E, 33.4, 52 A,

[56] References Cited UNITED STATES PATENTS 2,824,836 2/1958 Smith et al. 252/32.7 E 2,964,473 12/1960 Hughes et al. 252/33.4 X 3,219,666 11/1965 Norman et a1 252/51.5 A X 3,368,972 2/1968 Otto' 252/47.5 3,377,281 4/1968 Gower 252/32.7 E 3,591,497 7/1971 Walker 252/75 X Primary Examiner-Patrick P. Garvin Assistant Examiner-Andrew l-l. Metz Attorney, Agent, or FirmG. F. Magdeburger; C. J. Tonkin [57] ABSTRACT Functional fluid lubricating oil compositions are provided which comprise (A) a major amount of an oil of lubricating viscosity, and (B) an effective amount of each of the following: (1) an alkyl succinimide, (2) a Group 11 metal salt of a dihydrocarbyl dithiophosphoric acid, (3) a hydroxy fatty acid ester of a dihydric or polyhydric alcohol or oil-soluble alkoxylated derivatives thereof, and (4) a Group 11 metal salt of a hydrocarbyl sulfonic acid. Such lubricating composi- -tions are useful as functional fluids in systems requiring fluid coupling, hydraulic fluid and/or lubrication of relatively moving parts. The lubricating compositions of the invention are particularly useful as the functional fluid in automatic transmissions, particularly in passenger automobiles. In addition, the fluids do not form stable emulsions with water.

7 Claims, No Drawings DEMULSIFIED EXTENDED LIFE FUNCTIONAL FLUID BACKGROUND OF THE INVENTION 1. Field of the Invention This invention relates to lubricating oil compositions, particularly to lubricating oil compositions useful as functional fluids in systems requiring fluid coupling, hydraulic fluid, and/or lubrication of relatively moving parts. In a preferred embodiment, this invention relates to a lubricating oil composition useful as the functional fluid in automatic transmissions, particularly automatic transmissions used in passenger automobiles.

The trend today is towards longer and longer periods of time between servicing of the modern passenger automobile. This trend includes servicing of the automatic transmission. Automobile manufacturers, for the convenience of their customers, are seeking to extend the time between fluid changes in the automatic transmission to greater and greater mileages.

Automatic transmission fluids are required to have a variety of desirable characteristics besides acting as a satisfactory fluid coupling or torque converter. Among these are allowing the transmission to shift smoothly, allowing the transmission to lock up during a shift from one speed to another within a certain specified period of time, and lubricating relatively moving parts such as bearing surfaces and clutch plates.

An automatic transmission is a complicated piece of machinery. It includes a turbine drive unit with a torque converter and one or more clutches which are engaged and disengaged automatically by an intricate hydraulic control unit. In a typical automatic transmission the clutches are made up of alternating steel plates and steel plates faced on both sides with a friction material such as compressed paper.

To achieve a smooth shift, the clutch plates are not abruptly engaged, but are compressed together at a controlled rate, with pressure varying with speed and torque. Therefore, for a finite measurable period of time, the friction facings and steel surfaces are in relative motion until complete engagement occurs. The time elapsed between when shifting begins and relative motion between the plates ceases is called the time to lock up.

This time to lock up is an important specification to be met in qualifying an automatic transmission fluid for use in the transmission of an automobile manufacturer. In order to not cause a great strain on the drive train and obtain a smooth shift, maximum and minimum times to lock up are specified.

The functional fluid used in automatic transmissions is subjected to very severe conditions of use. The temperature of the automatic transmission fluid under normal operating conditions will reach 275F. Under more severe conditions, such as during climbing hills, trailer towing, stop-and-go traffic in the metroploitan areas, etc., the fluid temperature can increase significantly above this, up to, for example, 325F. and higher. In addition, the fluid is constantly being pumped and agitated, thereby being brought into initmate contact with the atmosphere within the automatic transmission.

Fresh air and atmospheric moisture are constantly introduced through the transmission housing breather tube. Under these conditions of high temperature and thorough mixing, the fluid tends to be oxidized, form- 0 ings are in relative motion to each other for a greater period of time, thereby allowing for the possiblity of greater wear higher clutch facing temperatures, and greater heat input to the fluid.

Eventually, the time to lock up will increase until it becomes too long to be acceptable. Prior to this point, the automatic transmission fluid must be changed to avoid permanent damage to clutches and/or bands.

In addition to the possibility of permanent damage to friction members, the degraded oil contains various contaminants which can either coagulate and settle out or plate out as a film throughout the transmission. This is particularly detrimental in the small passages and close fitting spool valves of the hydraulic control unit where a small amount of deposit can significantly change the size of the openings, cause sluggish valve movement thereby changing flow rates and pressures which, in turn, can markedly affect the performance of the entire transmission. In addition, should particules or lumps form in the fluid, they could completely block small openings such as in screens or filters and totally impair the function of the transmission.

In addition to possessing the necessary properties for use in an automatic transmission, the fluid must sometimes exhibit special properties because of conditions exisiting at the point of assembly and initial filling of the transmission.

During assembly and testing of transmissions at some assembly plants, large quanties of the fluid are spilled or otherwise escape from the transmission. This fluid is recovered and reused. Unfortunately, with age of the assembly facilities has come problems. One of these problems includes water leaks into the fluid recovery system. Before reuse of the recovered fluid, the water and other foreign materials must be removed. This is accomplished by passing the fluid through water separation and filtration facilities.

However, the additives present in the fluid tend to promote forming stable or semistable emulsions of the oil and water, a totally unacceptable situation. Accordingly, fluids to be used for initial fill of automatic transmissions in assembly facilities having a water problem in the fluid recovery system, must exhibit all the properties for long service life between changes. They must also not form emulsions or must form unstable emulsions which break relatively fast. The fluids of this invention are intended to meet these requirements.

2. DESCRIPTION OF THE PRIOR ART The use of amines and amine salts including hydroxyalkyl amines in lubricting compositions is known. See Stuart and Lowe, US. Pat. No. 2,758,086. Lubricating oil compositions containing heterocyclic nitrogen-containing detergent polymers, oil-soluble salts of aminoimides of long-chain mono-substituted polymeric hydrocarbyl succinic anhydrides and thiophosphates are described in Henderson et al., US. Pat. No. 3,265 ,6 l 8. The use of metal salts of phosphorodithioic acid to improve the oxidative stability of lubricating compositions has been often disclosed. See, for example, Mein- 3 hardt, U.S. Pat. No. 3,347,790, and Rutherford et al., U.S. Pat. No. Re.22,829. The combination of N,N-dialkyl aminoalkylene alkenyl succinimides and metal-di-' thiophoshphates are disclosed as being good detergent combinations in crankcase lubricating oils which pre-- vent the formation of sludges and varnishes without contributing to the deposit of large amounts of ash in the combustion chamber are described in Anderson et al., U.S. Pat. No. 3,018,247. Lubricating Oil Compositions suitable for use as automatic transmission fluids are described in Butler et al., U.S. Pat. No. 3,396,109. These compositions, which contain the reaction product of a dihydrocarbyl phosphonidithioic acid with an amine, are described as oxidation inhibitors and anitwear agents. Lube oil compositions containing a basic alkaline earth metal petroleum sulfonate, a copolymer of C-vinyl pyridine and an alkyl methacrylate, and a succinimide of mono(polyolefin)- succinic anhydride and a polyalkylene polyamine have been described as useful as turbine oils, gear oils, etc., in Henderson, U.S. Pat. No. 3,438,897. These compositions can optionally contain zinc dialkyl dithiophosphate.

SUMMARY OF THE INVENTION The lubricating oil compositions of this invention comprise (a) a major amount of an oil of lubricating viscosity, and (b) an effective amount of each of the following: (i) an alkenyl succinimide, (2) a Group II metal salt of a dihydrocarbyl dithiophosphoric acid, (3) a hydroxy fatty acid ester ofdihydric or polyhydric alcohol or oil-soluble alkoxylated derivatives thereof, and (4) a Group II metal salt of a hydrocarbyl sulfonic acid. These lubricating oil compositions are useful as the functional fluids in systems requiring fluid coupling, hydraulic fluids and/or lubrication of relatively moving parts. These fluids are particularly valuable since their useful life is significantly greater than functional fluids currently available.

DESCRIPTION OF INVENTION As described above, the extended life functional fluid compositions of this invention comprise a major amount of an oil of lubricating viscosity and an effective amount of each of an alkenyl succinimide, a Group II metal salt of a dihydrocarbyl dithiophosphoric acid, a hydroxy fatty acid ester, and a Group II metal salt of a hydrocarbyl sulfonic acid.

The alkenyl succinimide is present to, among other things, act as a dispersant and prevent formation of deposits formed during operation of the system containing the functional fluid. Alkenyl succinimides are well known. They are the reaction product of a polyolefin polymer-substituted succinic anhydride with an amine, preferably a polyalkenyl polyamine. The polyolefin polymer-substituted succinid anhydries are obtained by the reaction of a polyolefin polymer or a derivative thereof with maleic anydride. The succinic anhydride thus obtained is reacted with the amine. The preparation of the alkenyl succinimides has been described many times in the art. See, for example, U.S. Pat. No. 3,390,082 in Cols. 2 through 6, wherein such a description is set forth. Many of the alkenyl succinimides prepared by the techniques set forth therein are suitable for use in the present invention.

Particularly good results are obtained with the lubricating oil compositions of this invention when the alke- 4 nyl succinimide is derived from a polyisobutene substituted succinic anhydride anapolyalylene polyamine.

The polyisobutene from which the polyisobutene substituted succinic anhydride is derived is obtained from the polymerization of isobutene and can vary widely in its compositions. The average number of carbon atoms can range from 30 or less to 250 or more, with a resulting average. molecular weight of about 400 or less to 3,000 or more. Preferably, the average number of carbon atoms per polyisobutene molecule will range from about 50 to about with the polyisobutenes having a number average molecular weight of about 600 to about 1,500. More preferably, the average number of carbon atoms per polyisobutene molecule ranges from about 60 to about 90, and the number average molecular weight range from about 800 to about l,300. The polyisobutene is reacted with maleic anhydride according to well-known procedures to yield the polyisobutene substituted succinic anhydride.

The substituted succinic anhydride is reacted with a polyalkylene polyamine to yield the corresponding succinimide. Each alkylene radical of the polyalkylene polyamine usually has up to about 8 carbon atoms. The number of alkylene radicals can range up to about 8. The alkylene radical is exemplified by ethylene, propylene, butylene, trimethylene, tetramethylene, pentamethylene, hexamethylene, octamethylene, etc. The number of amino groups generally, but not necessarily, is one greater than the number of alkylene radicals present in the amine, i.e., if a polyalkylene polyamine contains 3 alkylene radicals, it will usually contain 4 amino radicals. The number of amino radicals can range up to about 9. Preferably, the alkylene radical contains from about 2 to about 4 carbon atoms and all amine groups are primary or secondary. In this case the number of amine groups exceeds the number of alkylene groups by 1. Preferably the polyalkylene polyamine contains from 3 to 5 amine groups/Specific examples of the polyalkylene polyamines include ethylenediamine, diethylenetriamine, triethylenetetramine, propylenediamine, tripropylenetetramine, tetracthylenepentamine, trimethylenediamine, pentaethylenehexamine, di-(trimethylene)-triamine, tri-(hexamethylene)-tetraamine, etc.

Other amines suitable for preparing the alkenyl succinimide useful in this invention include the cyclic amines such as piperizine, morpholine and dipiperizines.

Preferably the alkenyl succinimides used in the compositions of this invention have the following formula:

/0 R' -CH-- c l )u-Alk lene-m H I cu -q l n wherein: v

a. R, represents an alkenyl group, preferably a substantially saturated hydrocarbon derived from the polymerization of aliphatic mono-olefins. Preferably R, is derived from isobutene and has an average number of carbon atoms and a number average molecular weight as described above.

b. the. Alkylene" radical represents a substantially hydrocarbyl group containing up to about 8 carbon atoms and preferably containing from about 2-4 carbon atoms as'described hereinabove.

c. A represents a hydrocarbyl group, an amine-substituted hydrocarbyl group, or hydrogen. The hydrocarbyl group and the amine-substituted hydrocarbyl groups are generally the alkyl and amino-substituted alkyl analogs of the alkylene radicals described above. Preferably A represents hydrogen,

d. n represents an integer of from about 1 to l0, and preferably from about 3-5.

The alkenyl succinimide is present .in .the lubricating oil compositions of the invention is an amount effective to act as a dispersant and prevent the deposit of contaminants formed in the oil during operation of the system containing the functional fluid. This effective amount can vary widely and is relatively high compared to the levels of alkenyl succinimide normally usedin lubricating oils. For example, the amount of alkenyl succinimde can range from about 1.4 percent to about 4 percent weight of the total lubricating oil composition. Preferably the amount of alkenyl succinimide present in the lubricating oil composition of the invention ranges from about 1.75 to about 2.25 percent by weight of the total composition.

As set forth above, the lubricating oil compositions of the invention contain a Group II metal salt of a dihydrocarbyl dithiophosphoric acid. One function of this salt is to act as an oxidation inhibitor thereby preventing the formation of a variety of oxygenated hydrocarbon products which impair the usefulness and shorten the useful life of the lubricating oil.

As stated above, the temperatures to which the function fluids of automatic transmissions are subjected are often severe. Under these thermally severe conditions, not only is the lubricating oil quite prone to oxidation, but antioxidant additives quite often undergo thermal degradation. Accordingly, for a functional fluid to have an extended useful life, the oxidation inhibitor added to the lubricating oil must have good thermal stability at these relatively high temperatures, or its thermal degradation products must also exhibit antioxidation properties.

It has now been found that the above-mentioned Group ll metal salts of dihydrocarbyl dithiophosphoric acids exhibit the antioxidant and thermal stability properties required for the severeservice proposed. Group ll metal salts of phosphorodithioic acids have been described previously. See, for example, US. Pat. No. 3,390,080, cols. 6 and 7, wherein these compounds and their preparation are described generally. Suitably, the Group ll metal salts of the dihydrocarbyl dithiophosphon'c acids useful in the lubricating oil composition of this invention contain from about 4 to about 12 carbon .atoms, preferably from about 6 to about 12 carbon wherein: Q

e. R and R each independently represent hydrocarbyl radicals as described above, and

f. M, represents a Groupll metal cation as described above.

The dithiophosphoric salt is present in the lubricating oil compositions of this invention in an amount effective to inhibit the oxidation of the lubricating oil. This effective amount can vary widely and typically ranges from about 0.5 to about 1.5 percent by weight of the total composition, preferably the salt is present in an amount ranging from about 0.75 to about 1.0 percent by weight of the total lubricating oil composition.

The hydroxy fatty acid ester contained in the lubricating oil compositions of the invention principally acts as a friction modifier to give the lubricating oil the proper frictional charcteristics. These frictional characteristics are particularly important where the functional fluid is to be used in automatic transmissions. The frictional properties of the oil are an important factorin how the oil lubricated clutch plates lock up during shifting. Each manufacturer of automatic transmissions specifies certain lock-up characteristics for the transmissions it manufactures. Various friction modifiers are introduced into the functional fluid to give the oil the proper characteristics to meet the shift feel requirements of various manufacturers. The friction modifiers contained in the lubricating oil compositions of the present invention are particularly suited to maintain the friction characteristics desired by General Motors Corporation over an extended service interval.

The hydroxy fatty acid esters of the lubricating oil of the present invention are selected from hydroxy fatty acid esters of dihydric or polyhydric alcohols or oilsoluble oxyalkylenated derivatives thereof.

The fatty acid moiety must be of sufficient length to make the ester oil soluble. Suitably, the fatty acid moiety contains from 14 to 20 carbon atoms exclusive of alkoxylation, which can be in.a branched, but preferably are in a predominately straight chain containing from zero to one, preferably one, site of olefinic unsaturation. The fatty acid moiety is conveniently derived from naturally occurring substances. For example, castor oil is predominately a triglyceride in which the esterified acids are more than percent monoand dihydroxy-substituted 18 carbon atom acids with O-l sites of olefinic unsaturation.

in a preferred embodiment of this invention, the hydroxy'fatty acid ester has one of the following formulae:

$0 In CH R c--o---R IV 0 a CH -,C O y-R O R O-)- H wherein:

g. R represents an alkylene, preferably substantially straight chain, containing from 12 to 18 carbon atoms h. R represents the remainder of a dihydric or polyhydric alcohol containing from 2 to 5 carbon atoms and l to 3 hydroxyl groups;

i. R represents the remainder of a dihydric or trihydric alcohol containing 2 to 3 carbon atoms;

j. R represents an alkylene preferably containing from 2 to 3 carbon atoms such as ethylene or propylene. lf 2 represents an integer greater than 1, R can represent mixtures of alkylenes. Preferably, R does not represent mixed alkylenes;

k. x represents 1 or 2, preferably 1;

l. y represents 2 to 3, preferably 3; and

m. 2 represents an integer from 0 to 22, preferably 1 to 17.

As the number of oxyalkylene groups contained in the compounds of Formula lV increases, the oil solubility of the ester is reduced. Accordingly, it is preferred that the total number of oxyalkylene groups be no more than 22. This is conveniently determined by the hydroxyl number of the compound. This number is determined by reacting te compound with acetic anhydride and then titrating the acetic acid produced with potassium hydroxide. The hydroxyl number is expressed as the number of milligrams of potassium hydroxide needed to neutralize the acetic acid produced by one gram of the compound reacted with the acetic anhydride. Compounds of Formula IV useful in the fluids of this invention preferably are those in which y represents 3, R contains about 16 carbon atoms, R, represents ethylene, and the compound has a hydroxyl number of from 100 to 160. In these compounds, 2 has an average value of about 1 to about 7.

As discussed above, the fatty acid moiety can be derived from natural sources which yield fatty acids of the requisite carbon content. An excellent source of fatty acids for the preparation of the compounds of Formula III is castor oil. The ricinoleic acid derived therefrom can be esterified with various, dihydric and polyhydric alcohols such as ethylene glycol, propylene glycol, glycerol and pentaerythritol.

An excellent source of the compounds of Formula IV is castor oil. The hydroxyl groups of the ricinoleic acid can be oxyalkylenated with various alkylene oxides such as ethylene oxide or propylene oxide. The molecular weight, hydroxyl number and oil solubility can be controlled by the number of moles of alkylene oxide added to a mole of castor oil. Generally, the compounds useful in the invention are adducts containing not more than 22 moles of alkylene oxide per mole of castor oil.

Hydroxy fatty acid esters which have been found to be highly useful in the compositions of this invention include compositions available under the tradename FLEXRICIN, particularly numbers 9-17 and compositions available under the tradename SURFAC- TOL, particularly numbers 318 and 340, all of which are available for Baker Castor Oil Company.

Generally, the proper shift feel is obtained when the composition contains from 0.l to about 0.8 percent weight and preferably from about 0.2 to about 0.6 percent weight hydroxy fatty acid ester based on the total composition.

As stated above, the lubricating oil compositions of the invention contain a Group II metal salt of a hydrocarbyl sylfonic acid. One of the functions of this salt is to act as a detergent and dispersant. Among other things it prevents the deposit of contaminants formed 8 during high temperature operation of the system containing the functional fluid.

The Group II metal salts of hydrocarbyl sulfonic acids are well known. Many of these salts have been used as additives to lubricating oil'compositions. These salts comprise the neutralization product obtained by reacting a Group II metal base with the product obtained by treating a hydrocarbon oil with sulfuric acid. The resulting oil-derived sulfonic acid, when neutralized with the Group ll metal compound, yields the sulfonate which forms part of the composition of this invention.

Several processes for preparing these sulfonates are briefly outlined in U.S. Pat No. 2,395,7l3. Other processes are also discussed in US. Pat. No. 2,388,677.

The hydrocarbon portion of the sulfonate used in the lubricating oil compositions of the invention is derived from a hydrocarbon oil stock or synthetic organic moieties such as alkylated aromatics. Being derived from such a material the hydrocarbon moiety is a mixture of difi'erent hydrocarbyl groups, the specific composition of which depends upon the particular oil stock which was used as the starting material. The fraction of the oil stock which becomes sulfonated is predominantly an aliphatic-substituted carbocyclic ring. The sulfonic acid group attaches to the carbocyclic ring. The carbocyclic ring is predominantly aromatic in nature, although a certain amount of the cycloaliphatic content of the oil stock will also be sulfonated. The aliphateic substituent of the carbocyclic ring affects the oil solubility and detergency properties of the sulfonate. Suitably, the aliphatic substituent contains from about 12 to about 30 carbon atoms, and preferably from about 20 to 25 carbon atoms. The aliphatic substituent can be a straight or branched chain and can contain a limited number of oleflnic linkages, preferably less than 5 percent of the total carbon-to-carbon bonds are unsaturated.

The Group II metal cation of the sulfonate suitably is magnesium, calcium, strontium, barium, or zinc, and preferably is magnesium, calcium, or barium. Most preferably the Group II metal is calcium.

Preferably the Group I metal salt of a hydrocarbylsulfonic acid has the following formula:

0 0 II I a -s-o-n -o-sl-a 0 0 wherein:

n. each R represents a hydrocarbyl group as described above, and

o. M, represents a Group II metal cation as described above.

The group II metal salts of hydrocarbyl sulfonic acids are present in the lubricating oil compositions of the invention in an amount effective to prevent the deposit of contaminants formed in the oil during severe high temperature operation of the system containing the composition. This effective amount can vary widely and typically ranges from about 0.9 percent to about 1.8 percent weight, preferably from about 1.0 to about 1.4 percent weight of the total lubricating oil composition.

AUTOMATIC TRANSMISSION FLUIDS In a preferred embodiment the compositions of this invention are particularly suited for use in automatic transmissions, particularly in passenger automobiles. Automatic transmission fluids generally have a viscosity in the range from about 75 to 1,000 SUS (Saybolt Universal Seconds) at 100F. and from about 35 to 75 SUS at 2 1 1 The base oils for the automatic transmission fluids are light lubricating oils and ordinarily have a viscosity in the range of about 50 to 400 SUS at 100F. and 33 to 50 SUS at 210F. The base stock is a lubricating oil fraction of petroleum, eithernaphthenic or paraffinic base, unrefined, acid refined, hydrotreated or solvent refined as required in the particular lubricating need. Also, synthetic oils meeting the necessary viscosity requirements, either with or without viscosity index improvers, may be used as the base stock.

To summarize, the various constituents will be present in the automatic transmission fluid as follows. The alkenyl succinimide used in this invention generally will be present on the functional fluid in from about 1.4 to about 4 percent weight, more usually from about 1.75 to about 2.25 percent weight. In concentrates prepared for addition to the base oil prior to use, the alkenyl succinirnide can be present in from about to about 35 weight percent. The Group II metal salt of a dihydrocarbyl dithiophosphoric acid will generally be present in the functional fluid in from about 0.5 to about 1.5 percent weight, more usually from abut 0.75 to about 1.0 percent weight. The dithiophosphoric acid salts may be present in concentrates from about 5 to about 20 percent weight. The hydroxy fatty acid esters will generally be present in the functional fluid in from about 0.1 to about 0.8 percent weight, more usually from about 0.2 to about 0.6 percent weight. The amine may be present in concentrates in from about 2 to about 6 percent weight. The group 11 metal salt of hydrocarbyl sulfonic acid will generally be present in the functional fluid in from about 0.9 to about 1.8 percent weight, more usually from about 1.0 to about 1.4 percent weight. The sulfonic acid salt may be present in concentrates from about 5 to about 15 percent weight.

The functional fluid will normally contain a large number of other additives. It is usually necessary to heavily compound such oils in order to meet the exacting requirements specified.

Included among the other additives which can be used are additional oxidation inhibitors, such as, for example, the adduct obtained by combining terpene and phosphorous pentasulfide. Suitable materials are commerically available under the trade names Santolube and l-Iitec available from Monsanto Company and Edwin L. Cooper, Ltd. respectively.

Also commonly used in functional fluids are antifoam agents such as various fluorosilicone compounds commercially available. A particularly good antifoam agent is available from Dow Corning under the name FS 1265 Fluid.

Another useful functional fluid additive is a seal swell agent. A variety of compounds are useful for this function and include the bottoms product from catalytic cracking units used in the production of gasolines. These materials, containing a high percentage of condensed ring aromatics, are commerically available from Lubrizol Corporation under the name Lubrizol 725.

Also included in functional fluids are viscosity improving agents which are normally high molecular weight polymers such as the acrylate polymers. Useful examples include the copolymers of alkyl methacrylate with vinyl pyrrolidine available under the tradename Acryloid from Rohm & Haas and terpolymers derived from stryene, alkylacrylates and nitrogen-containing polymer precursors available from Lubrizol Corporation under the name Lubrizol 3,700 Series and methacrylates available from Texaco, Inc. Other viscosity improving agents include hydrocarbon polymers such as polyisobutylene or ethylene/propylene copolymers.

These additives will be present in the functional fluid in varying amounts necessary to accomplish the purpose for which they were included For example, additional oxidation inhibitors such as the terpene-phosophorous pentasulfide adduct may be present in amounts ranging from about 0.1 percent to about 1 percent weight or more. The fluorosilicone antifoam agent, for example, will generally be present in from about 2 to about 50 ppm. The viscosity index improver will normally be present in from about 0.5 to about 15 percent by weight of the base oil, more usually from about 2 to about 10 percent by weight of the base oil. The seal swell agent will be present in an amount effective to control the size of the seals with which the functional fluid comes in contact. For example, the bottoms from the catalytic cracking unit will be present in an amount ranging from about 1 to about 10 percent, more usually from about 2 to about 5 percent weight.

Other additives include pour point depressants, antisquawk agents, etc. Numerous automatic transmission fluid additives are listed in US. Pat. Nos. 3,156,652, and 3,175,976, which disclosure is incorporated herein by reference.

These various additives are also often incorporated into the concentrates and will be present therein corespondingly higher concentrations.

EXAMPLES The following examples are offered by way of illustration and not by way of limitation.

EXAMPLE 1 Demulsibility Testing Procedure The following is a test procedure for determining the demulsifibility of the fluids of this invention. Automatic transmission fluids approved for use in General Motors automatic transmissions must pass this test.

200 milliliters of the test oil at F. is placed in a Waring blender CC 8 W Model 1174. The blender is operated at the lowest speed for 30 seconds at which time 20 milliliters of distilled water is added. The blender is operated at the same speed for an additional 60 seconds. The oil-water mixture is then placed in a 400-ml. breaker which is covered with a watch glass and placed in a constant temperature oven set at F. The rate of water separation, oil clarity, water clarity, and interface layer condition are observed at 2, 4 and 24 hours.

FLUID COMPOSITION Table I shows the composition of a base fluid from which fluids in accordance with this invention can be prepared.

Quantity in Base Fluid Component Commercially available styrenc/ alkylacrylate/nitrogencontaining polymer precursor terpolymer Alkenyl succinimidc derived by reacting a polyisobutcne (number average molecular weight about 950) substituted succinic anhydride with tetracthylcnepentaminc; mole ratio of amine to anhydride 0.87 Zinc dioctyl dithiophosphate derived from mixed primary octanols Neutral calcium salt of a hydrocarbyl sulfonic acid prepared from a neutral lubricating oil Antifoam agent commercially available fluorosilicon Seal Swell Agent commercially available hydrocarbon obtained as a bottoms cut from the stream from a catalytic cracking unit used to produce gasoline; predominately condensed ring aromatic compounds Eastern base oil having aviscosity of 109 SUS at 100F and 40 SUS at 2l0F l mM/kg 8 mM/kg ppm to make I00 71 W Table II shows the results of demulsibility testing of several fluids of the invention (Fluids l6). These fluids were prepared by adding the materials indicated in the Table to the base fluid shown in Table I. Fluid No. 7 is a currently approved fluid which lasts 475 hours in the AT-l2 test described in Example II. However, as shown, it will not pass the demulsibility test and is not acceptable for use in plants having a water problem in the transmission assembly facilities.

12 Example II). The fluid numbers refer to the oils in Table II.

Table lll Compatibility testing Fluid 2 Hours 4 Hours 24 Hours 8. A W 12 20 20 O I98 200 200 E O O O 9. A l W O 7 20 O 20 20 200 E 200 193 0 10. A 2 W I0 20 20 O 20 200 200 E 190 O O l l. A 3 W 0 0 20 O 20 20 200 E 200 200 0 l2. A 4 W 0 10 20 O 20 20 200 E 200 I90 0 Oils l-4 in Table II are compatible with the currently approved automatic transmission. These results demonstrate that not only do the fluids of this invention possess the required degree of demulsibility but also exhibit th requisite compatibility.

EXAMPLE 2 General Motors AT-l2 Test Fluids proposed for use in General Motors automatic transmissions must pass a simulated use conditions test designated AT- 12 or Low Energy Cycling Test (LECT) 1970 Re-Revision.

The AT-l 2 test involves cycling a 350 cubic inch displacement General Motors engine driving a dynamometer-loaded Chevrolet Powerglide two-speed automatic Table ll Dcmulsibility Test Results Additives to Fluid of Table l 2 Hours 4 Hours 24 Hours l. glyceryl monoricinoleatc 0.4 7: W W 20 20 20 O 200 200 200 E 0 0 0 2. glyceryl monoricinoleate 0.4 W W 20 20 20 O 200 200 200 E 0 0 0 3. ethylene oxide adduct of castor oil; W 20 20 20 OH value 112. 0.2 7: W plus coco- O 200 200 200 nut oil fatty alkyl diethanol amine, E O 0 0 0.2 W 4. adduct of No. 3. 0.3 W plus amine of W 20 20 20 No. 3, 0.2 7: W O 200 200 200 E 0 0 0 5. ethylene oxide adduct of castor oil; W l0 I5 20 OH value 149. 0.2 7c W plus amine of 0 l0 10 200 No. 3, 0.2 k W E 200 195 O 6. penterythritol monoricinoleate 0.2 K: W W 10 20 20 O 10 200 200 E 200 O 0 7. coconut oil fatty alkyl diethanol W 0 0 5 amine 0.2 7: W O 0 0 25 E 220 220 l "W Water. 0 Oil. E Emulsion *Volume in milliliters of various phases COMPATIBILITY TESTING Fluids which pass the demulsibility test above must be compatible in this test with other approved fluids in order to receive Genral Motors approval. This is determined by mixing ml of the test fluid with 100 ml of an approved fluid and testing the mixture in the demulsification test. Table III shows the results of compatibility testing several fluids. Fluid A is a currently approved DEXRON" fluid available from Humble. This fluid approved for 225 hours use in the AT-l 2 test (see 13 takes place and includes a down-shift into L. At the end of seconds when engine speed has reached about 1,100 rpm, the throttle is opened and the cycle is repeated.

This cycled test is continued 24 hours per day, generally interrupted only mechanical difi'lculties, a shutdown for 24 hours at about 150 test hours, and weekend layovers. The time to lockup during the shift from L0 to Drive is measured regularly. Initial lockup mut be in the range of 0.375 to 0.6 seconds. The useful life of the fluid is considered spent when lock-up time exceeds 0.80 seconds. Current standards set by General Motors require the 0.80-second lock-up time not be reached for at least 225 hours.

Oil No. l of Table II was subjected to this test. A lock-up time of 0.6 seconds was reached after 436 hours of operation.

The above data demonstrate the long useful life of the functional fluids of this invention when placed in service in passenger autombile automatic transmissions. The useful life of the functional fluid tested above in the very severe AT-l2 test exceeded the useful life specified by Genral Motors for such fluids to used in transmissions manufactured by that company by 194 percent. This greatly extended useful life will allow greater oil drain intervals and thereby reduced operating costs for the owner of the vehicle.

While the invention has been described in detail and with reference to specific embodiments, it will be obvious other variations and embodiments can be effected within the spirit and scope of the appended claims.

We claim:

1. A lubricating oil composition which comprises:

A. a major amount of an oil of lubricating viscosity,

B. a dispersant amount of an alkenyl succinimide of a polyalkylene polyamine,

C. an antioxidant amount of a Group ll metal salt of a dihydrocarbyl dithiophosphoric acid,

D. a friction modifying amount of a hydroxy fatty acid ester of a dihydric or polyhydric alcohol or an oil-soluble oxalkylated hydroxy fatty acid ester of a dihydric or polyhydric alcohol, and

E. a detergent amount of a Group II metal salt of a hydrocarbylsulfonic acid.

2. A lubricating oil composition of claim 1 wherein (1) said alkenyl substituent of said succinimide is derived from polyisobutene, (2) said hydrocarbyl groups of said dithiophosphoric acid contain from 4 and 12 carbon atoms, (3) said fatty alkyl group of said hydroxy fatty acid contains from 14 to carbon atoms, and (4) said Group I] metal of said Group II metal salt of a hydrocarbylsulfonic acid is magnesium, calcium or barrum.

3. A lubricating oil composition of claim 1 wherein (I) said alkenyl succinimide has the following formula:

0 R -CH c:

l N(-AlkyleneN-) l-l CH c wherein:

a. R, represents an alkenyl group,

b. the Alkylene radical contains from 1 to 8 carbon atoms,

c. A represents a hydrocarbyl'group, an amine-substituted hydrocarbyl group or hydrogen, and

d. n represents an integer of from 1 to 10;

14 2. said dithiophosphoric acid salt has the following formula: ll

wherein:

e. R and R each independently represent hydrocarbyl radicals, and f. M, represents a Group II metal cation; 3. said hydroxy fatty acid ester has one of the following formulae:

- 0 III ca -R c o R wherein:

g. R represents a hydrocarbyl radical containing 12 to 18 carbon atoms and zero to one site of olefinic unsaturation;

h. R represents the remainder of a dihydric or polyhydric or polyhydric alcohol containing from 2 to 5 carbon atoms and from 2 to 4 hydroxy] groups,

i. R represents the remainder of a dihydric or trihydric alcohol containing 2 to 3 carbon atoms;

j. R represents an alkylene containing 2 to 3 carbon atoms;

k. x represents 1 or 2,

l. y represents 2 or 3, and m. 2 represents an integer from 0 to 22 such that the total number of R-,O-' groups is from I to 22; 5 and 4 4. said Group ll metal salt of a hydrocarbylsulfonic acid has the following formula:

h. x represents 1,

i. y represents 3,

j. 2 represents 1 to 17, and

k. M represents magnesium, calcium or barium.

5. A lubricating oil composition of claim 4 wherein:

a. said alkylene radical contains two carbon atoms,

b. n represents 4,

c. R and R each represent a hydrocarbyl radical containing 8 carbon atoms,

d. the group Cri (OH),--COO is derived from castor oil, and

e. M represents calcium.

6. A lubricating oil composition of claim 5 wherein said composition contains 1. from 1.4 to 4 percent weight of said alkenyl succinimide,

2. from 0.5 to 1.5 percent weight of said dithiophosphoric acid salt,

3. from 0.1 to 0.8 percent weight of said hydroxy fatty acid esters or oil-soluble oxyalkylated hydroxy fatty acid esters, and

4. from 0.9 to 1.8 percent weight of said Group ll metal salt of a hydrocarbylsulfonic acid.

7. A lubricating oil composition of claim 6 wherein said composition contains 1. from 1.75 to 2.25 percent weight of said alkenyl succinimide,

2. 0.75 to 1.0 percent weight of said dithiophosphoric acid salt,

3. from 0.2 to 0.6 percent of said hydroxy fatty acid esters or oil-soluble oxyalkylated hydroxy fatty acid esters, and

4. from 1.0 to 1.4 percent weight of said Group II metal salt of hydrocarbylsulfonic acid. 

1. A LUBRICATING OIL COMPOSITION WHICH COMPRISES: A. A MAJOR AMOUNT OF AN OIL OF LUBRICATING VISCOSITY, B. A DISPERSANT AMOUNT OF AN ALKENYL SUCCINIMICE OF A POLYALKENYLENE POLYAMIDE, C. AN ANTIOXIDANT AMOUNT OF A GROUP II METAL SALT OF A DIHYDROCARBYL DITHIOPHOSPHORIC ACID, D. A FRICTION MODIFYING AMOUNT OG OF A DIHYDRIC ALCOHOL OR AN OIL-SOLUBLE OXALKYLATED HYDROXY FATTY ACID ESTER OF A DIHYDRIC OR POLYHYDRIC ALCOHOL, AND E. A DETERGENT AMOUNT OF A GROUP 11 METAL SALT OF A HYDROCARBYLSULFONIC ACID.
 2. A lubricating oil composition of claim 1 wherein (1) said alkenyl substituent of said succinimide is derived from polyisobutene, (2) said hydrocarbyl groups of said dithiophosphoric acid contain from 4 and 12 carbon atoms, (3) said fatty alkyl group of said hydroxy fatty acid contains from 14 to 20 carbon atoms, and (4) said Group II metal of said Group II metal salt of a hydrocarbylsulfonic acid is magnesium, calcium or barium.
 2. 0.75 to 1.0 percent weight of said dithiophosphoric acid salt,
 2. from 0.5 to 1.5 percent weight of said dithiophosphoric acid salt,
 2. said dithiophosphoric acid salt has the following formula: II
 3. said hydroxy fatty acid ester has one of the following formulae:
 3. from 0.1 to 0.8 percent weight of said hydroxy fatty acid esters or oil-soluble oxyalkylated hydroxy fatty acid esters, and
 3. from 0.2 to 0.6 percent of said hydroxy fatty acid esters or oil-soluble oxyalkylated hydroxy fatty acid esters, and
 3. A lubricating oil composition of claim 1 wherein (1) said alkenyl succinimide has the following formula:
 4. from 1.0 to 1.4 percent weight of said Group II metal salt of hydrocarbylsulfonic acid.
 4. from 0.9 to 1.8 percent weight of said Group II metal salt of a hydrocarbylsulfonic acid.
 4. A lubricating oil composition of claim 3 wherein: a. R1 represents an alkenyl group derived from polyisobutene, b. said alkylene radical contains from 2 to 4 carbon atoms, c. A represents hydrogen, d. n represent 3, 4 or 5, e. R2 and R3 each represent a hydrocarbyl radical containing from 4 to 12 carbon atoms, f. M1 represents zinc, g. R4 represents a hydrocarbyl radical containing 14 to 16 carbon atoms and one site of olefinic unsaturation, h. x represents 1, i. y represents 3, j. z represents 1 to 17, and k. M2 represents magnesium, calcium or barium.
 4. said Group II metal salt of a hydrocarbylsulfonic acid has the following formula:
 5. A lubricating oil composition of claim 4 wherein: a. said alkylene radical contains two carbon atoms, b. n represents 4, c. R2 and R3 each represent a hydrocarbyl radical containing 8 carbon atoms, d. the group CH3-R4 (OH)x-COO is derived from castor oil, and e. M2 represents calcium.
 6. A lubricating oil composition of claim 5 wherein said composition contains
 7. A lubricating oil composition of claim 6 wherein said composition contains 